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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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KIT DE FÉRULAS SEMIRRÍGIDAS 4 UDS. — 4 UDI-DI variants, MDR

MD Atlas
FABRICACION DE EMERGENCIAS SANITARIAS,S.L.

Data from EUDAMED, last updated May 23, 2026

KIT DE FÉRULAS SEMIRRÍGIDAS 4 UDS.

8436600744000PTT

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: FABRICACION DE EMERGENCIAS SANITARIAS,S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8436600744000PTT
Device name: KIT DE FÉRULAS SEMIRRÍGIDAS 4 UDS.
Device model: 4000P
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: FABRICACION DE EMERGENCIAS SANITARIAS,S.L.
SRN: ES-MF-000013283
Country: Spain
Email: patricia@fesa-fabricante.com
Phone: +34 986 26 50 19

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KS89WBMZ8RWHXRNM6JMKKV3B

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

4000BPR84366007400604
4000PG84366007404282
4000PP84366007404428
4000P84366007404732